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- Marfan syndrome - Symptoms and causes - Mayo Clinic
Marfan syndrome is an inherited disorder that affects connective tissue — the fibers that support and anchor your organs and other structures in your body Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton
- Marfan Syndrome: Symptoms, Causes Treatment - Cleveland Clinic
Many people with Marfan syndrome develop changes in their heart and blood vessels Marfan syndrome (MFS) is a genetic condition that makes your connective tissue too loose and elastic Connective tissue typically provides strength and flexibility to many structures in your body
- Marfan syndrome - Wikipedia
Marfan syndrome is caused by mutations in the FBN1 gene on chromosome 15, [33] which encodes fibrillin 1, a glycoprotein component of the extracellular matrix Fibrillin-1 is essential for the proper formation of the extracellular matrix, including the biogenesis and maintenance of elastic fibers
- Marfan syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
The two primary features of Marfan syndrome are vision problems caused by a dislocated lens (ectopia lentis) in one or both eyes and defects in the large blood vessel that distributes blood from the heart to the rest of the body (the aorta)
- Marfan Syndrome and Related Aortic Conditions - Stanford Health Care
The central mission of our center has always been to be an integrated, multidisciplinary unit that provides comprehensive, cost-effective, state-of-the-art diagnostic evaluation and care for adult and pediatric patients with Marfan syndrome and Aortic disorders
- Marfan Syndrome – Symptoms and Causes | Penn Medicine
Marfan syndrome is a genetic disorder that affects connective tissue in the body Explore Marfan syndrome symptoms, causes, risk factors, and treatments
- Marfan syndrome - Johns Hopkins Medicine
Marfan syndrome is a rare genetic disorder of the connective tissue, affecting the skeleton, lungs, eyes, heart and blood vessels The condition is caused by a defect in the gene that tells the body how to make fibrillin-1, often from a parent who is also affected
- Marfan Syndrome - Marfan Foundation
About 1 in 5,000 people have Marfan syndrome, including men and women of all races and ethnic groups About 3 out of 4 people with Marfan syndrome inherit it, meaning they get the genetic mutation from a parent who has it
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